ABOUT SAMSUNG BIOLOGICS
Samsung Biologics is a full-service provider offering development and cGMP manufacturing services. We deliver a broad range of services from development and manufacturing to fill and finish, covering both clinical molecules and commercial products. Established in April 2011, Samsung Biologics will transform the global healthcare industry over the next decade through our quality, technology and innovation. Our facilities are custom designed for monoclonal & recombinant production with maximum flexibility. Our one-stop services include cell line generation, process and analytical method development, analytical services (characterization, comparability, IPC, lot release & stability), and clinical and commercial bulk cGMP manufacturing of drug substance and drug product. We also provide quality assurance and quality control services, as well as worldwide regulatory compliance standards & support for our customers. We are centrally located in the heart of Asia, within 20 minutes of Incheon International Airport.
CONTACT INFORMATION
Samsung Biologics
300 Songdo Bio Way, Yeonsu-gu
Incheon, 21987
KOREA, REPUBLIC OF
Phone: +82 32 455 3114
Contact: Jinyong Kim
BROCHURES
- Link Your Antibody To Its Fullest Potential
- Plant 5 - Dream Plant: Within Your Reach. Built For Your Success.
- Super Plant 4
- CDO Services: Agile. Flexible. Focused On You.
- Why Samsung Biologics?
- Trusted End-To-End CDMO Partner For Your Journey
- Antibody Drug Conjugates: Link Your Antibody To Its Fullest Potential
- The Power Of One: mRNA Services
- Aseptic Fill/Finish Service
- Leveraging Proprietary CDO Platforms
- Capacity To Secure Your Success
FEATURED ARTICLES
- Mitigating Early Development Risks
- Improving Therapeutic Protein Efficacy Through Charge Profile Adjustment
- Leveraging Optimized Transient Expression For Material Generation And Early Stage Insight
- Embracing Quality-By-Design For Enhanced Development Strategies
- Streamlining Single-Use Assemblies In The Bulk-Fill Step Of Downstream Processing
- Reducing ADC Timelines With Integrated Development And Manufacturing Services
- Accelerating The Development And Production Of High-Quality bsAbs
- Optimizing Sialic Acid Clone Screening
- Addressing And Adapting To Evolving mRNA Market Trends
- β-Glucan As A Process-Related Impurity In Biopharmaceuticals
- Monoclonal Antibody Manufacturing: Build Or Outsource?
- Biopharma Tech Transfer: Facility Fit And Process Gap Assessments
- Choose A Partner That Integrates Market Intelligence For Aseptic Fill/Finish
- Beyond COVID-19: How Localization Strengthens Supply Chains
- The Challenges Of Biopharmaceutical Quality
- Why Choosing The Right CDMO Partner Is Essential In Today's Market
- Overcome Data Integrity Challenges In Biopharma Production
- Setting The Right Goals: Go Digital, Not Paperless
- Single-Use Manufacturing Systems: Implementation Considerations
- Ensuring Quality And Safety Through Process Optimization, Characterization
WEBINARS
- Navigating Challenges During Formulation Development
- Formulation Considerations For The Development Of High Concentration Biopharmaceuticals
- Harnessing Analytical Development To Empower Process Development For Successful Manufacturing
- Downstream Strategies To Accelerate Preclinical Development Timelines
- All Eyes On mRNA: Addressing Key Insights Into The Next Blockbuster
- Biopharmaceutical Process Characterization
- Accelerated Tech Transfer For A COVID-19 Program
- Continuous Manufacturing: Challenges, Advantages Of N-1 Perfusion
- How COVID-19 Is Redefining Drug Development And Manufacturing
- Key Considerations When Outsourcing An Aseptic Fill/Finish Project To A CMO Partner